戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 nd three InDels in four KI mice but not in a control mouse.
2 ands from the transgenic mouse versus virgin control mouse.
3 ced efficiency compared to v-Ras-transformed control mouse 3T3 and p50-deficient cells.
4 cating that at least two different promoters control mouse Abcg2 transcription during hematopoiesis.
5 erstitial macrophages (NAMs) are required to control mouse-adapted SARS-CoV-2 (MA-10) infection.
6 cted from uninfected ticks and from negative control mouse and human bloods, and these background DNA
7 latory devices to growth cytokine targets to control mouse and primary human T-cell proliferation.
8   Importantly, NKp46 recognition of ecto-CRT controls mouse B16 melanoma and RAS-driven lung cancers
9 ine whether cholinergic signaling in the SNc controls mouse behavior, we used optogenetics in awake b
10  found that all four PARs are present in the control mouse bladder, and follow a unique distribution.
11      Our data suggest that Rab11a critically controls mouse blastocyst development and soluble matrix
12 mentin, while those in comparable regions of control mouse brain did not.
13 ed glycan structures in wild-type littermate control mouse brains.
14 s seen in the transgenic mouse model but not control mouse brains.
15  novel social competition with an unfamiliar control mouse but had no effect on an established hierar
16 he Serine/Threonine kinases PIM1 and PIM2 in controlling mouse CD8 T lymphocyte antigen receptor-medi
17  from HVCN1-deficient mice mirrored those in control mouse cells treated with Zn(2+).
18                      Through comparison with control mouse cells, we have identified differentially e
19  exon junction complex (EJC) that binds RNA, controls mouse cerebral cortical size by regulating NSC
20             Significant QTLs are detected to control mouse cholesterol gallstone formation.
21 rize key transcriptional regulatory elements controlling mouse Daf1 expression, a 2.5-kb fragment cor
22                                 Pups born to control mouse dams were suckled from birth to postnatal
23 e results uncover a crucial role of Brpf1 in controlling mouse embryo development and regulating cell
24 tivates mTORC1 activity in both p18(-/-) and control mouse embryonic fibroblast cells, suggesting tha
25 m the pharyngeal apparatus with the heart in control mouse embryos and when Tbx1, the gene for 22q11.
26  to electrically stimulated heart tubes from control mouse embryos or embryos with the Na+-Ca2+ excha
27 low)) and 774 +/- 135 Crry molecules/cell on control mouse erythrocytes.
28 tional phenotypes that distinguish them from control mouse fibroblasts.
29 identified in a screen to uncover genes that control mouse gametogenesis.
30 arisons of the transcriptomes of mGEPs and a control mouse gastric epithelial cell line revealed that
31           Compared with a normoxic, chow-fed control mouse heart, hypoxia decreased PPARalpha express
32 osin heavy chain in adult Gsalpha-DF but not control mouse hearts was reversed by cTnI overexpression
33 ptive metabolic changes caused by hypoxia in control mouse hearts were found to have occurred already
34 use hearts compared with wild-type (Npr1+/+) control mouse hearts.
35 thesis were measured in 9-week-old ob/ob and control mouse hearts.
36 mban, and 0.26 +/- 0.01 mumol/L in wild-type control mouse hearts.
37 s 187 +/- 12 micron2, P < .05) compared with control mouse hearts.
38  that one or more microRNAs (miRNA) known to control mouse hematopoiesis and lineage commitment might
39 e components of the molecular circuitry that controls mouse hematopoiesis and suggest that other micr
40 nvestigate whether B cells are important for controlling mouse hepatitis virus strain A59 infection,
41 wed reduced oxygen consumption compared with control mouse hepatocytes.
42 h), saturable, and substantial compared with control mouse IgG.
43 re randomized to treatment with CNTO 1081 or control mouse IgG.
44 metabolism of SUR1 knock-out (SUR1(-/-)) and control mouse islets with d-[U-(13)C]glucose as substrat
45  differential gene expressions in mutant and control mouse kidneys.
46 of hepatic glycogen synthesis in the ADM and control mouse liver in vivo were measured using new adva
47  isolated from Foxa2(loxP/loxP) Alfp.Cre and control mouse livers, and HNF6 binding to its target, Gl
48 go]-CLIP) sequencing in miR-122 knockout and control mouse livers, as well as in matched human hepato
49 subset of retinal ganglion cells (RGCs) that controls mouse looming-evoked defensive responses throug
50 ng tissues from those of i.d.-inoculated and control mouse lung tissues.
51                         Since the airways of control mouse lungs contain few alcian blue/periodic aci
52 ell influx between bleomycin-treated CKO and control mouse lungs.
53 ur screen reveals individual APA events that control mouse melanoma growth in an immunocompetent host
54       Here we study this question in a novel controlled mouse melanoma model that enables us to explo
55 icantly enhanced its therapeutic efficacy in controlling mouse melanoma (8-fold reduction in tumor vo
56 of these genes in vivo and provides a novel, controlled mouse model for spontaneous venous thrombosis
57               Using a conscious, temperature-controlled mouse model, we showed that maintaining a cor
58 , we sought to assess whether data from well-controlled mouse models can compensate for scarce human
59 ison of tumor immune landscapes in carefully controlled mouse models.
60                                Compared with controls, mouse models of ischemia-reperfusion injury, u
61                                           In control mouse muscle, desmin is enriched at the sarcolem
62 urrence of trans-rearrangements in this well-controlled mouse mutant system and found a 50-100-fold i
63 ) with tunable physicochemical properties to control mouse myoblast growth and myotube formation.
64 ize as compared with the alpha-granules from control mouse platelets.
65 Syk Y342F mouse platelets when compared with control mouse platelets.
66 e in the levels of lactate between db/db and control mouse retina.
67 s has identified Sinc/Prni as the major gene controlling mouse scrapie incubation time.
68              Proteomic analysis of MR-/- and control mouse sera showed that an additional 4 out of 52
69                      Here, we show that RXRs control mouse serous-macrophage identity by regulating c
70 and lungs; PF and tissue samples from only 1 control mouse showed bacterial growth, and no control mi
71 aucomatous mouse strain, DBA/2J and a normal control mouse strain (C57BL/6) were used in the study.
72 abetes-prone NOD mice and compared it to the control mouse strain C57BL/6.
73  to equalize manganese levels between HD and control mouse striatal cells and rescued the ATM-p53 sig
74 xpress human CD4 on the surface, but not the control mouse T cells lacking human CD4.
75  and VI but more in layers II/III and V than control mouse TCAs.
76  implanted osmotic pumps, with an additional control mouse used for histologic examination (n = 1).